Nenad Blau

6PUBLICATIONS
20CO-AUTHORS
Infant and child healthProteomics and intermolecular interactions (excl. medical proteomics)Human biophysicsMedical biochemistry - proteins and peptides (incl. medical proteomics)Epigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Sep 16, 2026
Mechanisms of Aging in Phenylketonuria (PKU).

|Aug 25, 2026
A Contemporary Pathomechanistic Nosology of Inherited Lysosomal Disorders.

|Jun 21, 2026
Integrating Functional Consequence Annotation With PAH Allelic Phenotype Values Refines Prediction of Tetrahydrobiopterin Responsiveness.

|Oct 22, 2021
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation.

Dorothea Haas, Jana Hauke, Kathrin V Schwarz

|Jan 23, 2019
Phenylalanine hydroxylase variants interact with the co-chaperone DNAJC12.

Kunwar Jung-Kc, Nastassja Himmelreich, Karina S Prestegård

|Oct 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.

Diane B Zastrow, Heather Baudet, Wei Shen

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Frequent Collaborators

1 joint publications

Diane B Zastrow

1 joint publications

Wei Shen

1 joint publications

Selina S Dwight

1 joint publications

Matt W Wright